PMID- 21569380 OWN - NLM STAT- MEDLINE DCOM- 20110913 LR - 20211020 IS - 1471-2377 (Electronic) IS - 1471-2377 (Linking) VI - 11 DP - 2011 May 12 TI - Identification of peripheral inflammatory markers between normal control and Alzheimer's disease. PG - 51 LID - 10.1186/1471-2377-11-51 [doi] AB - BACKGROUND: Multiple pathogenic factors may contribute to the pathophysiology of Alzheimer's disease (AD). Peripheral blood markers have been used to assess biochemical changes associated with AD and mild cognitive impairment (MCI) and involved in their pathophysiology. METHODS: Plasma samples and clinical data were obtained from participants in the Ansan Geriatric Study (AGE study). Plasma concentrations of four candidate biomarkers were measured in the normal control (NC), MCI, and AD group: interleukin-8 (IL-8), IL-10, monocyte chemoattractant protein-1 (MCP-1), and tumor necrosis factor-alpha (TNF-alpha).Body mass index (BMI), MMSE (Mini Mental State Examination), CDR(Clinical Dementia Rating) score and homocystein level were recorded with social and demographic information. RESULTS: Total of 59 subjects were randomly selected for this analysis [NC (n = 21), MCI(n = 20) and AD(n = 18)]. In demographic data, educational year was correlated with the diagnosis states (p < 0.0001). No significant differences in cardiovascular disease, BMI and use of NSAIDs were found in MCI or AD group compared with NC group, respectively. The involvement of inflammatory illness or conditions in subjects, WBC count, fibrinogen and homocystein of the three groups, but no significant differences were found in each groups. The plasma IL-8 level was lower in MCI and AD patients compared with the normal control group (respectively, p < 0.0001). The MCI and AD patients had similar MCP-1, IL-10, and TNF-alpha level. CONCLUSIONS: Our study suggests the existence of an independent and negative relationship between plasma IL-8 levels and functional status in MCI and AD patients. FAU - Kim, Sam-Moon AU - Kim SM AD - Center for Biomedical Science, Division of Brain Diseases, National Institute of Health in Korea (KNIH), Osong Health Technology Administration Complex 643 Yeonje-ri, Gangoe-myeon, Chungcheongbuk-do, 363-951, Republic of Korea. FAU - Song, Juhee AU - Song J FAU - Kim, Seungwoo AU - Kim S FAU - Han, Changsu AU - Han C FAU - Park, Moon Ho AU - Park MH FAU - Koh, Youngho AU - Koh Y FAU - Jo, Sangmee Ahn AU - Jo SA FAU - Kim, Young-Youl AU - Kim YY LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20110512 PL - England TA - BMC Neurol JT - BMC neurology JID - 100968555 RN - 0 (Biomarkers) RN - 0 (Cytokines) RN - EC 1.14.99.1 (Cyclooxygenase 2) RN - EC 1.14.99.1 (PTGS2 protein, human) SB - IM MH - Aged MH - Aged, 80 and over MH - Alzheimer Disease/blood/*complications MH - Analysis of Variance MH - Biomarkers/blood MH - Cognition Disorders/blood/complications MH - Cyclooxygenase 2/*blood MH - Cytokines/*blood MH - Female MH - Follow-Up Studies MH - Humans MH - *Inflammation/blood/diagnosis/etiology MH - Male MH - Psychiatric Status Rating Scales MH - Random Allocation MH - Retrospective Studies PMC - PMC3120663 EDAT- 2011/05/17 06:00 MHDA- 2011/09/14 06:00 PMCR- 2011/05/12 CRDT- 2011/05/17 06:00 PHST- 2011/01/10 00:00 [received] PHST- 2011/05/12 00:00 [accepted] PHST- 2011/05/17 06:00 [entrez] PHST- 2011/05/17 06:00 [pubmed] PHST- 2011/09/14 06:00 [medline] PHST- 2011/05/12 00:00 [pmc-release] AID - 1471-2377-11-51 [pii] AID - 10.1186/1471-2377-11-51 [doi] PST - epublish SO - BMC Neurol. 2011 May 12;11:51. doi: 10.1186/1471-2377-11-51.